Regressive Events in Neurogenesis

Plasticity of ocular dominance columns in monkey striate cortex

Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,629

Physiology of nerve growth factor.

Thoenen, H., & Barde, Y. (1980) · Physiological Reviews · doi:10.1152/physrev.1980.60.4.1284 · Cited by 1,573

CELL DEATHS IN NORMAL VERTEBRATE ONTOGENY

Glucksmann, A. (1951) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.1951.tb00774.x · Cited by 1,208

The development of ocular dominance columns in normal and visually deprived monkeys

Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123

Proliferation, differentiation and degeneration in the spinal ganglia of the chick embryo under normal and experimental conditions

Hamburger, V., & Levi‐Montalcini, R. (1949) · Journal of Experimental Zoology · doi:10.1002/jez.1401110308 · Cited by 985

Selective growth stimulating effects of mouse sarcoma on the sensory and sympathetic nervous system of the chick embryo

Levi‐Montalcini, R., & Hamburger, V. (1951) · Journal of Experimental Zoology · doi:10.1002/jez.1401160206 · Cited by 958

Elimination of synapses in the developing nervous system

Purves, D., & Lichtman, J. W. (1980) · Science · doi:10.1126/science.7414326 · Cited by 808

Local control of neurite development by nerve growth factor

Campenot, R. B. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.10.4516 · Cited by 747

Prenatal development of the visual system in rhesus monkey

RAKIC, P. T., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0040 · Cited by 739

The Nerve Growth Factor: Biochemistry, Synthesis, and Mechanism of Action

Greene, L. A., & Shooter, E. M. (1980) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.03.030180.002033 · Cited by 734

Multiomic Analysis of Neurons with Divergent Projection Patterns Identifies Novel Regulators of Axon Pathfinding

Fernández‐Nogales, M., López-Cascales, M. T., Murcia‐Belmonte, V., Escalante, A., Fernández‐Albert, J., Muñoz‐Viana, R., Barco, Á., & Herrera, E. (2022) · Advanced Science · doi:10.1002/advs.202200615 · Cited by 24

Radiation‐Induced Apoptosis and Developmental Disturbance of the Brain*

Inouye, M. (1995) · Congenital Anomalies · doi:10.1111/j.1741-4520.1995.tb00296.x · Cited by 24

Complex patterns of [125I]ω-conotoxin GVIA binding site expression during postnatal rat brain development

Filloux, F. M., Schapper, A., Naisbitt, S. R., Olivera, B. M., & McIntosh, J. M. (1994) · Developmental Brain Research · doi:10.1016/0165-3806(94)90017-5 · Cited by 24

Basic fibroblast growth factor prevents neuronal death and atrophy of retrogradely labeled preganglionic neurons in vivo

Blottner, D., & Baumgarten, H. G. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90020-q · Cited by 24

Transient tectogeniculate projections in neonatal kittens: An autoradiographic study

Stein, B. E., McHaffie, J. G., Harting, J. K., Huerta, M. F., & Hashikawa, T. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902390406 · Cited by 24

Relationship between natural variations in motoneuron number and body size in Xenopus laevis: A test for size matching

Sperry, D. G. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902640209 · Cited by 24

Functional imaging in the assessment of capability for recovery after stroke

Heiss, W., Thiel, A., Winhuisen, L., Mühlberger, B., Kessler, J., & Herholz, K. (2003) · Journal of Rehabilitation Medicine · doi:10.1080/16501960310010115 · Cited by 23

Traumatic brain injury recapitulates developmental changes of axons

Song, H., Chen, C., Kelley, B. J., Tomasevich, A., Lee, H., Dollé, J.-P., Cheng, J., Garcia, B. A., Meaney, D. F., & Smith, D. H. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102332 · Cited by 25

Thalamo-cortical and cerebello-cortical functional connectivity in development

D’Andrea, C. B., Marek, S. A., Van, A. N., Miller, R. L., Earl, E., Stewart, S. B., Dosenbach, N. U. F., Schlaggar, B. L., Laumann, T. O., Fair, D. A., et al. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad198 · Cited by 23

The BDNF Val66Met polymorphism (rs6265) enhances dopamine neuron graft efficacy and side-effect liability in rs6265 knock-in rats

Mercado, N. M., Stancati, J. A., Sortwell, C. E., Mueller, R. L., Boezwinkle, S. A., Duffy, M. F., Fischer, D. L., Sandoval, I. M., Manfredsson, F. P., Collier, T. J., et al. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105175 · Cited by 23

Molecular characterization of NDRG4/Bdm1 protein isoforms that are differentially regulated during rat brain development

Nakada, N., Hongo, S., Ohki, T., Maeda, A., & Takeda, M. (2002) · Developmental Brain Research · doi:10.1016/s0165-3806(02)00303-6 · Cited by 23

Chapter 25 Arousal and locomotion: from schizophrenia to narcolepsy

García‐Rill, E., Reese, N. B., & Skinner, R. D. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61879-8 · Cited by 23

Postnatal development of the rat dorsal funiculus

Chung, K., & Coggeshall, R. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-04-00972.1987 · Cited by 23

Growth and neurotrophic factors regulating development and maintenance of sympathetic preganglionic neurons

Schober, A., & Unsicker, K. (2001) · International review of cytology · doi:10.1016/s0074-7696(01)05002-1 · Cited by 23

Apoptosis in the basal ganglia of the developing human nervous system

Itoh, K., Suzuki, K., Bise, K., Itoh, H., Mehraein, P., & Weis, S. (2001) · Acta Neuropathologica · doi:10.1007/s004010000252 · Cited by 23

Transient cortical pathways in the pyramidal tract of the neonatal ferret

Meissirel, C., Dehay, C., & Kennedy, H. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903380205 · Cited by 23

Control of cell number in the developing neocortex. I. Effects of early tectal ablation

Pallas, S. L., Gilmour, S. M., & Finlay, B. L. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90148-4 · Cited by 23

Trigeminotectal and other trigeminofugal projections in neonatal kittens: An anatomical demonstration with horseradish peroxidase and tritiated leucine

McHaffie, J. G., Ogasawara, K., & Stein, B. E. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902490308 · Cited by 23

Growing together and growing apart: the non-genetic forces on children in the same family

Goodman, R. (1991) · Elsevier eBooks · doi:10.1016/b978-0-7506-0029-3.50019-4 · Cited by 23

Expression of surface glycoproteins early in leech neural development

McGlade‐McCulloh, E., Muller, K. J., & Zipser, B. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902990109 · Cited by 23

Normal numbers of retinotectal synapses during the activity-sensitive period of optic regeneration in goldfish: HRP-EM evidence implicating synapse rearrangement and collateral elimination during map refinement

Hayes, W., & Meyer, R. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-04-01400.1989 · Cited by 23

Applications of Nonlinear Dynamical Systems Theory in Developmental Psychology: Motor and Cognitive Development

Metzger, M. A. (1997) · Nonlinear Dynamics Psychology and Life Sciences · doi:10.1023/a:1022323926870 · Cited by 22

Intrinsically directed pruning as a mechanism regulating the elimination of transient collateral pathways

Tolbert, D. L. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90171-4 · Cited by 22

Contribution of Proton Magnetic Resonance Spectroscopy to the Evaluation of Children with Unexplained Developmental Delay

Martin, E., Keller, M., Ritter, S., Largo, R. H., Thiel, T., & Loenneker, T. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000180559.29393.be · Cited by 22

Cerebrocortical Microdysgenesis with Anomalous Callosal Connections: A Case Study in the Rat

Rosen, G. D., Galaburda, A. M., & Sherman, G. F. (1989) · International Journal of Neuroscience · doi:10.3109/00207458908987438 · Cited by 22

Sensory Processing by Novel, Experimentally Induced Cross‐Modal Circuitsa

Frost, D. O. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb48893.x · Cited by 22

Elimination of intramedullary axon collaterals of cat spinal ?-motoneurons following peripheral nerve injury

Havton, L. A., & Kellerth, J. ‐. (1990) · Experimental Brain Research · doi:10.1007/bf00228873 · Cited by 22

6 Nerve Growth Factor and the Issue of Mitosis in the Nervous System

BLACK, J., DiCicco-Bloom, E. M., & Dreyfus, C. F. (1990) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60087-3 · Cited by 22

Development of the spinal‐medullary projection from the mouse barrel field

Crandall, J. E., Whitcomb, J. M., & Caviness, V. S. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902390207 · Cited by 22

Second Messengers in Neuronal Growth and Degeneration

Mattson, M. P. (1990) · doi:10.1007/978-1-349-11922-6_1 · Cited by 22

Drosophila Corazonin Neurons as a Hub for Regulating Growth, Stress Responses, Ethanol-Related Behaviors, Copulation Persistence and Sexually Dimorphic Reward Pathways

Khan, Z., Tondravi, M., Oliver, R., & Vonhoff, F. (2021) · Journal of Developmental Biology · doi:10.3390/jdb9030026 · Cited by 20

Development of Segment- and Target-Related Neuronal Identity in the Medicinal Leech

Jellies, J., Kopp, D. M., & Bledsoe, J. W. (1992) · Journal of Experimental Biology · doi:10.1242/jeb.170.1.71 · Cited by 21

Neuroanatomical Bases of Hemispheric Functional Specialization in the Human Brain: Developmental Factors

Witelson, S. F. (1992) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4684-6805-2_7 · Cited by 21

The Effects of Early Focal Brain Injury on Lateralization of Cognitive Function

Stiles, J. (1998) · Current Directions in Psychological Science · doi:10.1177/096372149800700101 · Cited by 21

Neuronal degeneration and reorganization: a mutual principle in pathological and in healthy interactions of limbic and prefrontal circuits

Teuchert, G. (2000) · Springer eBooks · doi:10.1007/978-3-7091-6301-6_22 · Cited by 21

Histochemical observations on unique rod-like cells in the developing retina of the normal rat

Araki, M., Hanihara, T., & Saito, T. (1988) · Journal of Neurocytology · doi:10.1007/bf01674205 · Cited by 21

Maintenance of transient occipitospinal axons in the rat

Sharkey, M. A., Lund, R. D., & Dom, R. M. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90116-1 · Cited by 21

YVAD protect post-natal retinal ganglion cells against axotomy-induced but not free radical-induced axonal degeneration in vitro

Lucius, R., & Sievers, J. (1997) · Molecular Brain Research · doi:10.1016/s0169-328x(97)00170-8 · Cited by 20

Genetic influences on the spontaneous EEG: An examination of 15‐year‐old and 17‐year‐old twins

McGuire, K. A., Katsanis, J., Iacono, W. G., & McGue, M. K. (1998) · Developmental Neuropsychology · doi:10.1080/87565649809540698 · Cited by 21

Postnatal ontogeny of the rat brain neurotensin receptor mRNA

Hermans, E., Jeanjean, A. P., Laduron, P. M., Octave, J., & Maloteaux, J. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90639-3 · Cited by 21

Transient Expression of Opioid Receptors in Defined Regions of Developing Brain: Are Embryonic Receptors Selective?

Barg, J., & Simantov, R. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb06412.x · Cited by 21

Molecular and Cellular Aspects of Nerve Regeneratio

Schwartz, M. (1987) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238709083737 · Cited by 21

Induction of target-directed optic axon outgrowth: Effect of retinae transplanted to anophthalmic mice

Hankin, M., & Lund, R. D. (1990) · Developmental Biology · doi:10.1016/0012-1606(90)90183-j · Cited by 21

α2-Chimaerin Is Required for Eph Receptor-Class-Specific Spinal Motor Axon Guidance and Coordinate Activation of Antagonistic Muscles

Kao, T., Nicholl, G. C. B., Johansen, J. A., Kania, A., & Beg, A. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4151-14.2015 · Cited by 20

Long-Term Effect of Retinal Ganglion Cell Axotomy on the Histomorphometry of Other Cells in the Porcine Retina

Kom??romy, A. M., Brooks, D. E., Kallberg, M. E., Dawson, W. W., Sz??l, ?., Luk??ts, ?., Samuelson, D. A., Sapp, H. L., Gelatt, K. N., & Sherwood, M. B. (2003) · Journal of Glaucoma · doi:10.1097/00061198-200308000-00004 · Cited by 20

A high-throughput framework to detect synapses in electron microscopy images

Navlakha, S., Suhan, J. P., Barth, A. L., & Bar‐Joseph, Z. (2013) · Bioinformatics · doi:10.1093/bioinformatics/btt222 · Cited by 20

Comparative effects of alcohol and thiamine deficiency on the developing central nervous system

Bâ, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.07.015 · Cited by 20

Regionally Specific Distribution of Corticospinal Synapses Because of Activity-Dependent Synapse EliminationIn Vitro

Ohno, T., Maeda, H., & Sakurai, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3903-03.2004 · Cited by 20

Apoptosis in human embryo development: 3. Fas‐induced apoptosis in brian primary cultures

Nat, R., Radu, E., Regalia, T., & Popescu, L. M. (2001) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2001.tb00177.x · Cited by 20

From Superior Adaptation and Function to Brain Dysfunction—The Neglect of Epigenetic factors

Saugstad, L. F. (2004) · Nutrition and Health · doi:10.1177/026010600401800102 · Cited by 20

A mathematical model for the analysis of cross-sectional brain glucose metabolism data in children

Muzik, O., Janisse, J. J., Acer, J., Shen, C., Chugani, D. C., & Chugani, H. T. (1999) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(99)00018-4 · Cited by 20

Embryonic neuronal death due to neurotrophin and neurotransmitter deprivation occurs independent of Apaf-1

Honarpour, N., Tabuchi, K., Stark, J. M., Hammer, R. E., Südhof, T. C., Parada, L. F., Wang, X., Richardson, J. A., & Herz, J. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00275-5 · Cited by 20

BMP4- and RA-Induced Apoptosis Is Mediated through the Activation of Retinoic Acid Receptor α and γ in P19 Embryonal Carcinoma Cells

Glozak, M. A., & Rogers, M. B. (1998) · Experimental Cell Research · doi:10.1006/excr.1998.4075 · Cited by 20

Glial ontogeny and glial neoplasia: The search for closure

Linskey, M. E. (1997) · Journal of Neuro-Oncology · doi:10.1023/a:1005751018617 · Cited by 20

Target dependence of adult neurons: pattern of terminal arborizations

Marty, S., Weinitz, J., & Peschanski, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-09-05257.1994 · Cited by 20

Peripheral maps and synapse elimination in the cerebellum of the rat.I. Representation of peripheral inputs through the climbing fiber pathway in the posterior vermis of the normal adult rat

Mulle, C., Delhaye‐Bouchaud, N., & Mariani, J. (1987) · Brain Research · doi:10.1016/0006-8993(87)91290-x · Cited by 20

Cell death in the inner and outer nuclear layers of the developing retina in the wallaby setonix brachyurus (quokka)

Harman, A. M., Snell, L. L., & Beazley, L. D. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902890102 · Cited by 20

Ipsilateral retinal projections into the tectum during regeneration of the optic nerve in the cichlid fish Haplochromis burtoni: A dil study in fixed tissue

Wilm, C., & Fritzsch, B. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230608 · Cited by 20

Role of astroglial cell clones in the survival and differentiation of cerebellar embryonic neurons

Alliot, F., Delhaye‐Bouchaud, N., Geffard, M., & Pessac, B. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90223-4 · Cited by 20

Appearance of neuronal S-100β during development of the rat brain

Yang, Q., Hamberger, A., Wang, S., & Haglid, K. G. (1996) · Developmental Brain Research · doi:10.1016/0165-3806(95)00180-8 · Cited by 20

The Effects of Monocular Enucleation on Ganglion Cell Number and Terminal Distribution in the Ferret's Retinal Pathway

Thompson, I. D., Morgan, J. E., & Henderson, Z. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00503.x · Cited by 19

Development of ‘non-specific’ cholinesterase-containing neurons in the dorsal thalamus of the rat

Robertson, R. T., & Mostamand, F. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90168-x · Cited by 19

Cyclin‐dependent kinase 5 influences Rohon‐Beard neuron survival in zebrafish

Kanungo, J., Li, B., Zheng, Y.-L., & Pant, H. C. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04114.x · Cited by 19

Postnatal changes in the numerical density and total number of asymmetric and symmetric synapses in the hypoglossal nucleus of the rat

OʼKusky, J. R. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00048-0 · Cited by 19

Enhanced Purkinje cell survival in granuloprival cerebellar cultures

Seil, F. J. (1987) · Developmental Brain Research · doi:10.1016/0165-3806(87)90057-5 · Cited by 19

Humoral and surface-anchored factors in development and repair of the nervous system

Varon, S. S., Pettmann, B., & Manthorpe, M. (1988) · Progress in brain research · doi:10.1016/s0079-6123(08)60521-x · Cited by 19

5 Mechanisms of Programmed Cell Death in Caenorhabditis elegans and Vertebrates

Miura, M., & Yuan, J. (1996) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60427-5 · Cited by 19

Morphogenesis of catecholaminergic interneurons in the frog spinal cord

Heathcote, R. D., & Chen, A. B. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903420107 · Cited by 19

Development and Acquisition of Motor Skills: A Challenging Prospect for Neuroscience

Paillard, J. (1986) · Springer eBooks · doi:10.1007/978-94-009-4460-2_24 · Cited by 19

Trophic and Growth‐Regulating Mechanisms in the Central Nervous System Monitored by Intracerebral Neural Transplants

Gage, F. H., & Björklund, A. (2007) · Novartis Foundation symposium · doi:10.1002/9780470513422.ch9 · Cited by 19

Expression of Bcl-2 protein in murine neural cells in culture

Mizuguchi, M., Ikeda, K., Asada, M., Mizutani, S., & Kamoshita, S. (1994) · Brain Research · doi:10.1016/0006-8993(94)91064-2 · Cited by 19

Apoptotic cell death induced by serum and its prevention by thiols

Kurita, T., & Namiki, H. (1994) · Journal of Cellular Physiology · doi:10.1002/jcp.1041610109 · Cited by 19

Transient expression of somatostatin mRNA in the auditory system of neonatal rat

Sekitani, M., Shiosaka, S., Kuriyama, H., Lee, Y., Ikeda, M., & Tohyama, M. (1990) · Molecular Brain Research · doi:10.1016/0169-328x(90)90096-v · Cited by 19

Withdrawal of collaterals of sympathetic axons to the rat eye during postnatal development: the role of function

Vidovic, M., & Hill, C. E. (1988) · Journal of the Autonomic Nervous System · doi:10.1016/0165-1838(88)90154-3 · Cited by 19

Transplanted raphe and hippocampal fetal neurons do not displace afferent inputs to the dorsal hippocampus from serotonergic neurons in the median raphe nucleus of the rat

Zhou, F., Auerbach, S. B., & Azmitia, E. C. (1988) · Brain Research · doi:10.1016/0006-8993(88)91543-0 · Cited by 19

Transient expression of somatostatin messenger RNA and peptide in the hypoglossal nucleus of the neonatal rat

Seroogy, K. B., Bayliss, D. A., Szymeczek, C. L., Hökfelt, T. G. M., & Millhorn, D. E. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90053-l · Cited by 19

Response of retinal terminals to loss of postsynaptic target neurons in the dorsal lateral geniculate nucleus of the adult cat

Pearson, H. E., Stoffler, D. J., & Sonstein, W. J. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903150308 · Cited by 19

Postnatal development of crossed and uncrossed corticorubral projections in kitten: A PHA‐L study

Higashi, S., Yamazaki, M., & Murakami, F. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902990305 · Cited by 19

Developmental Disability in the Young and Postoperative Cognitive Dysfunction in the Elderly After Anesthesia and Surgery: Do Data Justify Changing Clinical Practice?

Cottrell, J. E., & Hartung, J. (2012) · Mount Sinai Journal of Medicine A Journal of Translational and Personalized Medicine · doi:10.1002/msj.21283 · Cited by 18

Crossed–uncrossed projections from primate retina are adapted to disparities of natural scenes

Gibaldi, A., Benson, N. C., & Banks, M. S. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2015651118 · Cited by 18

Induction of programmed cell death in a dorsal root ganglia × neuroblastoma cell line

Linnik, M. D., Hatfield, M. D., Swope, M. D., & Ahmed, N. K. (1993) · Journal of Neurobiology · doi:10.1002/neu.480240403 · Cited by 18

Postnatal changes in the uncrossed retinal projection of pigmented and albino syrian hamsters and the effects of monocular enucleation

Thompson, I. D., Cordery, P. M., & Holt, C. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903570202 · Cited by 18

Formation of an ipsilateral corticospinal tract after ablation of cerebral cortex in neonatal rat

Ono, K., Yamano, T., & Shimada, M. (1991) · Brain and Development · doi:10.1016/s0387-7604(12)80131-8 · Cited by 18

Effects of target deprivation on the morphology and survival of adult dorsal column nuclei neurons

Marty, S., & Peschanski, M. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903560404 · Cited by 18

Histological and electron microscopic milestones in the development of the retina of a marsupial wallaby, Macropus eugenii

Spira, A. W., & Marotte, L. R. (1989) · Anatomy and Embryology · doi:10.1007/bf00315699 · Cited by 18

Maintenance of targeting errors by isthmo‐optic axons following the intraocular injection of tetrodotoxin in chick embryos

Péquignot, Y., & Clarke, P. G. H. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903210304 · Cited by 17

Chapter 16 Exogenous administration of neuronotrophic factors in vivo protects central nervous system neurons against axotomy induced degeneration

Varon, S. S., Williams, L. R., & Gage, F. H. (1987) · Progress in brain research · doi:10.1016/s0079-6123(08)61824-5 · Cited by 18

Fine structural alteration in target-deprived axonal terminals in the rat thalamus

Marty, S., & Peschanski, M. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90348-4 · Cited by 18

A ciliary neuronotrophic factor from peripheral nerve and smooth muscle which is not retrogradely transported

Smet, P. J., Abrahamson, I. K., Ressom, R. E., & Rush, R. A. (1991) · Neurochemical Research · doi:10.1007/bf00965546 · Cited by 18

Local glycolysis fuels actomyosin contraction during axonal retraction

Santos, R., Lokmane, L., Ozdemir, D., Traoré, C., Agesilas, A., Hakibilen, C., Lenkei, Z., & Zala, D. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202206133 · Cited by 18

Development of dissociated cryopreserved rat cortical neurons in vitro

Schock, S., Jolin‐Dahel, K., Schock, P. C., Theiss, S., Arbuthnott, G. W., Garcia-Munoz, M., & Staines, W. A. (2012) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2012.01.016 · Cited by 17

Cell death organizes the postnatal development of the trigeminal innervation of the cerebral vasculature

O’Connor, T. P., & van der Kooy, D. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90248-8 · Cited by 17

Effect of prenatal ethanol exposure on postnatal neural gene expression in the rat

Naus, C. C. G., & Bechberger, J. F. (1991) · Developmental Genetics · doi:10.1002/dvg.1020120406 · Cited by 17

Phosphorus-31 magnetic resonance brain spectroscopy of children at risk for a substance use disorder: Preliminary results

Moss, H. B., Talagala, S. L., & Kirisci, L. (1997) · Psychiatry Research Neuroimaging · doi:10.1016/s0925-4927(97)00067-x · Cited by 17

The supraoptic nucleus: a morphological and quantitative study in control and hypophysectomised rats.

Crespo, D., Ramos, J., González, C., & Fernández‐Viadero, C. (1990) · Europe PMC (PubMed Central) · Cited by 17

Morphology of HRP-labelled cochlear nerve axons in the dorsal cochlear nucleus of the developing hamster

Schweitzer, L., & Cecil, T. (1992) · Hearing Research · doi:10.1016/0378-5955(92)90056-s · Cited by 17

Shifting retinal maps in the development of the lateral geniculate nucleus

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